反应 #1824302

ord-500a69e1de044357914b0e51f8ae6535

反应方程式

CC(=NOCc1ccccc1-n1c(Cl)nn(C)c1=O)c1cccc(C(F)(F)F)c1
5-chloro-2, 4-dihydro-2-methyl-4-[2-[[[[1-[3(trifluoromethyl)phenyl]-ethylidene]amino]oxy]methyl]phenyl]- 3H-1,2,4-triazol-3-one
CC(=NO)c1cccc(C(F)(F)F)c1
1-[3-(trifluoromethyl)phenyl]ethanone oxime
[K+].[OH-]
KOH
[H-].[Na+]
NaH
CC(C)(C)[O-]
t-butoxide
COc1nn(C)c(=O)n1-c1ccccc1CON=C(C)c1cccc(C(F)(F)F)c1
2,4-dihydro-5-methoxy-2-methyl-4-[2-[[[[1-[3-(trifluoromethyl)phenyl]-ethylidene]amino]oxy]methyl]phenyl]- 3H-1,2,4-triazol-3-one

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Examples of the combined processes of Steps 2 and 3 include the reaction of 5-chloro-2, 4-dihydro-2-methyl-4-[2-[[[[1-[3(trifluoromethyl)phenyl]-ethylidene]amino]oxy]methyl]phenyl]- 3H-1,2,4-triazol-3-one with 1-[3-(trifluoromethyl)phenyl]ethanone oxime in the presence of a base (e.g., KOH, NaH or K t-butoxide) in a suitable solvent (e.g., THF) and the subsequent reaction of the product of that reaction with methanol in the THF solution to form 2,4-dihydro-5-methoxy-2-methyl-4-[2-[[[[1-[3-(trifluoromethyl)phenyl]-ethylidene]amino]oxy]methyl]phenyl]- 3H-1,2,4-triazol-3-one; the reaction of 5-chloro-2, 4-dihydro-2-methyl-4-[2-[[[[1-[3(trifluoromethyl)phenyl]-ethylidene]amino]oxy]methyl]phenyl]- 3H-1,2,4-triazol-3-one with 1-[3,5-(bistrifluoromethyl)phenyl]ethanone oxime in the presence of a base and the subsequent reaction of the product of that reaction with methanol to form 5-chloro-2, 4-dihydro-2-methyl-4-[2-[[[[1-[3(trifluoromethyl)phenyl]-ethylidene]amino]oxy]methyl]phenyl]-3H-1,2,4-triazol-3-one.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USH0001809uspto-grants-1999_10